Canonical Allele Identifier: CA1033970302
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1682440844
gnomAD v3: 2-96143507-A-G
gnomAD v4: 2-96143507-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143507A>G , CM000664.2:g.96143507A>G GRCh38
NC_000002.11:g.96809246A>G , CM000664.1:g.96809246A>G GRCh37
NC_000002.10:g.96172973A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*316T>C MANE Select ENSP00000288943.4:n.*316T>C
ENST00000288943.4:c.*316T>C ENSP00000288943.4:n.*316T>C
NM_004418.3:c.*316T>C NP_004409.1:n.*316T>C
XM_017003546.1:c.*316T>C XP_016859035.1:n.*316T>C
NM_004418.4:c.*316T>C MANE Select NP_004409.1:n.*316T>C
Search 100 bp 5'
Search 100 bp 3'